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Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation
Brassinosteroids (BRs), plant steroid hormones, play important roles in plant cell elongation and differentiation. To investigate the mechanisms of BR signaling, we previously used the BR biosynthesis inhibitor Brz as a chemical biology tool and identified the Brz-insensitive-long hypocotyl4 mutant...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515986/ https://www.ncbi.nlm.nih.gov/pubmed/28720789 http://dx.doi.org/10.1038/s41598-017-06016-2 |
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author | Yamagami, Ayumi Saito, Chieko Nakazawa, Miki Fujioka, Shozo Uemura, Tomohiro Matsui, Minami Sakuta, Masaaki Shinozaki, Kazuo Osada, Hiroyuki Nakano, Akihiko Asami, Tadao Nakano, Takeshi |
author_facet | Yamagami, Ayumi Saito, Chieko Nakazawa, Miki Fujioka, Shozo Uemura, Tomohiro Matsui, Minami Sakuta, Masaaki Shinozaki, Kazuo Osada, Hiroyuki Nakano, Akihiko Asami, Tadao Nakano, Takeshi |
author_sort | Yamagami, Ayumi |
collection | PubMed |
description | Brassinosteroids (BRs), plant steroid hormones, play important roles in plant cell elongation and differentiation. To investigate the mechanisms of BR signaling, we previously used the BR biosynthesis inhibitor Brz as a chemical biology tool and identified the Brz-insensitive-long hypocotyl4 mutant (bil4). Although the BIL4 gene encodes a seven-transmembrane-domain protein that is evolutionarily conserved in plants and animals, the molecular function of BIL4 in BR signaling has not been elucidated. Here, we demonstrate that BIL4 is expressed in early elongating cells and regulates cell elongation in Arabidopsis. BIL4 also activates BR signaling and interacts with the BR receptor brassinosteroid insensitive 1 (BRI1) in endosomes. BIL4 deficiency increases the localization of BRI1 in the vacuoles. Our results demonstrate that BIL4 regulates cell elongation and BR signaling via the regulation of BRI1 localization. |
format | Online Article Text |
id | pubmed-5515986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55159862017-07-19 Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation Yamagami, Ayumi Saito, Chieko Nakazawa, Miki Fujioka, Shozo Uemura, Tomohiro Matsui, Minami Sakuta, Masaaki Shinozaki, Kazuo Osada, Hiroyuki Nakano, Akihiko Asami, Tadao Nakano, Takeshi Sci Rep Article Brassinosteroids (BRs), plant steroid hormones, play important roles in plant cell elongation and differentiation. To investigate the mechanisms of BR signaling, we previously used the BR biosynthesis inhibitor Brz as a chemical biology tool and identified the Brz-insensitive-long hypocotyl4 mutant (bil4). Although the BIL4 gene encodes a seven-transmembrane-domain protein that is evolutionarily conserved in plants and animals, the molecular function of BIL4 in BR signaling has not been elucidated. Here, we demonstrate that BIL4 is expressed in early elongating cells and regulates cell elongation in Arabidopsis. BIL4 also activates BR signaling and interacts with the BR receptor brassinosteroid insensitive 1 (BRI1) in endosomes. BIL4 deficiency increases the localization of BRI1 in the vacuoles. Our results demonstrate that BIL4 regulates cell elongation and BR signaling via the regulation of BRI1 localization. Nature Publishing Group UK 2017-07-18 /pmc/articles/PMC5515986/ /pubmed/28720789 http://dx.doi.org/10.1038/s41598-017-06016-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yamagami, Ayumi Saito, Chieko Nakazawa, Miki Fujioka, Shozo Uemura, Tomohiro Matsui, Minami Sakuta, Masaaki Shinozaki, Kazuo Osada, Hiroyuki Nakano, Akihiko Asami, Tadao Nakano, Takeshi Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title | Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title_full | Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title_fullStr | Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title_full_unstemmed | Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title_short | Evolutionarily conserved BIL4 suppresses the degradation of brassinosteroid receptor BRI1 and regulates cell elongation |
title_sort | evolutionarily conserved bil4 suppresses the degradation of brassinosteroid receptor bri1 and regulates cell elongation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515986/ https://www.ncbi.nlm.nih.gov/pubmed/28720789 http://dx.doi.org/10.1038/s41598-017-06016-2 |
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